日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Reliable ECG Anomaly Detection on Edge Devices for Internet of Medical Things Applications

面向医疗物联网应用的边缘设备可靠心电图异常检测

Hizem, Moez; Bousbia, Leila; Ben Dhiab, Yassmine; Aoueileyine, Mohamed Ould-Elhassen; Bouallegue, Ridha

Sustainable E-Health: Energy-Efficient Tiny AI for Epileptic Seizure Detection via EEG

可持续电子健康:用于通过脑电图检测癫痫发作的节能型微型人工智能

Hizem, Moez; Aoueileyine, Mohamed Ould-Elhassen; Belhaouari, Samir Brahim; El Omri, Abdelfatteh; Bouallegue, Ridha

Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities

颅面畸形作为综合征的基本诊断工具

Al Kaissi, Ali; Ryabykh, Sergey; Nassib, Nabil; Bouchoucha, Sami; Benjemaa, Lamia; Rejeb, Imen; Hizem, Syrine; Kenis, Vladimir; Grill, Franz; Kircher, Susanne Gerit; Shboul, Mohammad; Ben Chehida, Farid

A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report

戈谢病中GBA基因罕见的纯合p.Arg87Trp变异:病例报告

Jilani, Houweyda; Hsoumi, Faten; Rejeb, Imen; Elaribi, Yasmina; Hizem, Syrine; Sebai, Molka; Rolfs, Arndt; Benjemaa, Lamia

New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene

FAN1基因突变引起的核巨细胞间质性肾炎新家族病例

Rejeb, Imen; Jerbi, Mouna; Jilani, Houweyda; Gaied, Hanène; Elaribi, Yasmina; Hizem, Syrine; Aoudia, Raja; Hedri, Hafedh; Zaied, Chiraz; Abid, Salwa; Bacha, Hassen; BenAbdallah, Taieb; BenJemaa, Lamia; Goucha, Rim

Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

Beckwith-Wiedemann综合征:两例突尼斯患者的临床、组织病理学和分子研究及文献综述

Sassi, Hela; Elaribi, Yasmina; Jilani, Houweyda; Rejeb, Imen; Hizem, Syrine; Sebai, Molka; Kasdallah, Nadia; Bouthour, Habib; Hannachi, Samia; Beygo, Jasmin; Saad, Ali; Buiting, Karin; H'mida Ben-Brahim, Dorra; BenJemaa, Lamia

Repurposing of an old drug: In vitro and in vivo efficacies of buparvaquone against Echinococcus multilocularis

老药新用:布帕伐醌对多房棘球绦虫的体外和体内疗效

Rufener, Reto; Dick, Luca; D'Ascoli, Laura; Ritler, Dominic; Hizem, Amani; Wells, Timothy N C; Hemphill, Andrew; Lundström-Stadelmann, Britta

First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations

突尼斯人群中首例由VPS13B基因突变引起的科恩综合征病例报告

Rejeb, Imen; Jilani, Houweyda; Elaribi, Yasmina; Hizem, Syrine; Hila, Lamia; Zillahrdt, Julia Lauer; Chelly, Jamel; Benjemaa, Lamia

Vascular endothelial growth factor (VEGFA) gene variation in polycystic ovary syndrome in a Tunisian women population

突尼斯女性人群中多囊卵巢综合征患者的血管内皮生长因子(VEGFA)基因变异

Ben Salem, Assila; Megdich, Fatma; Kacem, Olfa; Souayeh, Malek; Hachani Ben Ali, Faten; Hizem, Sondes; Janhai, Faouzi; Ajina, Mounir; Abu-Elmagd, Muhammad; Assidi, Mourad; Al Qahtani, Mohammed H; Mahjoub, Touhami

Female mate choice can drive the evolution of high frequency echolocation in bats: a case study with Rhinolophus mehelyi

雌性择偶可以驱动蝙蝠高频回声定位的进化:以菊头蝠(Rhinolophus mehelyi)为例

Puechmaille, Sébastien J; Borissov, Ivailo M; Zsebok, Sándor; Allegrini, Benjamin; Hizem, Mohammed; Kuenzel, Sven; Schuchmann, Maike; Teeling, Emma C; Siemers, Björn M